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在 Flatiron 数据库中,对于转移性乳腺癌患者,使用哌柏西利联合芳香化酶抑制剂或单独使用芳香化酶抑制剂的真实世界治疗模式。

Real-world treatment patterns for palbociclib plus an aromatase inhibitor, or an aromatase inhibitor alone, for patients with metastatic breast cancer in the Flatiron Database.

机构信息

University of California San Francisco Comprehensive Cancer Center, San Francisco, California, USA.

Pfizer Inc., New York, New York, USA.

出版信息

Int J Cancer. 2024 Feb 15;154(4):701-711. doi: 10.1002/ijc.34748. Epub 2023 Oct 13.

Abstract

There are limited real-world comparative effectiveness data for palbociclib plus an aromatase inhibitor (AI) as a first-line (1L) treatment examining endpoints that require long term follow-up and post 1L progression. The Flatiron Health Analytic Database was used to characterize treatment and dosing patterns in patients with hormone receptor-positive/human epidermal growth factor 2-negative (HR+/HER2-) metastatic breast cancer (mBC) receiving palbociclib plus an AI vs an AI alone in routine US clinical practice. In addition, time to chemotherapy (TTC) and real-world progression-free survival (rwPFS) when combining 1L and second-line of therapy (rwPFS2) were assessed. Of 1324 patients who received palbociclib plus an AI between February 3, 2015 and March 31, 2020, 1110 (83.8%) started palbociclib at the recommended 125 mg/day dose. After stabilized inverse probability treatment-weighting (sIPTW), median TTC in patients treated with palbociclib plus an AI and AI alone was 37.4 months (95% confidence interval [CI], 33.7-40.7) and 29.2 months (95% CI, 26.8-33.5), respectively (hazard ratio [HR] = 0.77 [95% CI, 0.69-0.86], P < .0001); median rwPFS2 was 32.6 months (95% CI, 29.4-35.2) and 20.7 months (95% CI, 18.9-22.6), respectively (HR = 0.62 [95% CI, 0.54-0.70], P < .0001). Sensitivity analyses with propensity score matching showed similar results to sIPTW analyses. Results from this large real-world study examining additional effectiveness outcomes beyond 1L rwPFS and overall survival support the use of palbociclib plus an AI as a 1L treatment for patients with HR+/HER2- mBC.

摘要

在需要长期随访和一线治疗进展后评估的终点方面,帕博西利联合芳香化酶抑制剂(AI)作为一线(1L)治疗的真实世界比较疗效数据有限。使用 Flatiron Health 分析数据库描述了在常规美国临床实践中,接受帕博西利联合 AI 与单独 AI 治疗的激素受体阳性/人表皮生长因子受体 2 阴性(HR+/HER2-)转移性乳腺癌(mBC)患者的治疗和剂量模式。此外,评估了 1L 和二线治疗(rwPFS2)联合的化疗开始时间(TTC)和真实世界无进展生存期(rwPFS)。在 2015 年 2 月 3 日至 2020 年 3 月 31 日期间接受帕博西利联合 AI 治疗的 1324 例患者中,有 1110 例(83.8%)以推荐的 125mg/天剂量开始使用帕博西利。经过稳定的逆概率治疗加权(sIPTW)后,接受帕博西利联合 AI 和单独 AI 治疗的患者的中位 TTC 分别为 37.4 个月(95%置信区间 [CI],33.7-40.7)和 29.2 个月(95% CI,26.8-33.5)(风险比 [HR] = 0.77 [95% CI,0.69-0.86],P<0.0001);中位 rwPFS2 分别为 32.6 个月(95% CI,29.4-35.2)和 20.7 个月(95% CI,18.9-22.6)(HR = 0.62 [95% CI,0.54-0.70],P<0.0001)。倾向性评分匹配的敏感性分析结果与 sIPTW 分析相似。这项大型真实世界研究的结果表明,除了 1L rwPFS 和总生存期之外,还观察到了其他疗效终点,支持将帕博西利联合 AI 作为 HR+/HER2-mBC 患者的一线治疗。

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